
Gnaim Lab
@samergnaim
We are an enthusiastic organic chemistry research group at Weizmann Institute, situated at the interface of reaction discovery, electrosynthesis and catalysis
ID: 1213172467591569408
https://www.weizmann.ac.il/MCMS/gnaim/ 03-01-2020 18:57:25
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P(V) goes radical! Check out our work on P(V) functionalization that appeared in ChemRxiv today. A radical and stereoselective method to form new and exciting P-C bonds. A great collaboration between Baran Lab and BMS Martin Eastgate Martins S. Oderinde, Ph.D #realtimechem




In these hard days for us, some nice news: our recent work in Chemical Science about an employment of the nitrenium ions in electrophilic amination made it to the cover. Congratulations Kuldeep Singh @Idan_Avigdori Mark Gandelman. Link for the paper. pubs.rsc.org/en/content/art…


Excited to share our work that just appeared Angewandte Chemie. We introduce an orthogonal palladium(II) strategy to engineer complex modified proteins. We like transcription factors, so we demonstrated this approach in the preparation of 10 complex TF analogs onlinelibrary.wiley.com/doi/10.1002/an…


🎉 I am happy to share that in January, I'll open my new research group🧪⚗️at Technion Schulich Faculty of Chemistry, Technion Technion Israel Gratitude to my mentors Morandi Lab Shabat Group and my friends for their support🙏 We're looking for students and postdocs to join the lab origreenlab.com






Very proud to share our work where we reveal the composition & structure of the SEI on Na ion anodes using dynamic nuclear polarization! Getting us closer to mapping nm scale heterogeneous surface layers with NMR! Great work by Yuval Steinberg 👏👏👏🔋🧲🔋 pubs.acs.org/doi/10.1021/ja…

We are excited and thrilled to share that our research program has been awarded funding by European Research Council (ERC)! We're eager to dive into developing new borylation methodologies, utilizing unique boron species in combination with electrochemistry. Exciting times ahead!#ERCStG

We developed a novel reaction that enables a direct synthesis of amines from olefins via C=C bond cleavage. This process which we termed Triazenolysis represents an aza-version of ozonolysis reaction. Congrats to all involved Nature Chemistry Technion Israel nature.com/articles/s4155…



